Canonical Allele Identifier: CA436965752
Gene: GHSR HGNC NCBI

Linked Data

MyVariant Identifiers: chr3:g.172166162G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.172448372G>C , CM000665.2:g.172448372G>C GRCh38
NC_000003.11:g.172166162G>C , CM000665.1:g.172166162G>C GRCh37
NC_000003.10:g.173648856G>C NCBI36
NG_021159.1:g.5085C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000241256.3:c.42C>G MANE Select ENSP00000241256.2:p.Leu14=
ENST00000241256.2:c.42C>G ENSP00000241256.2:p.Leu14=
ENST00000427970.1:c.42C>G ENSP00000395344.1:p.Leu14=
NM_004122.2:c.42C>G NP_004113.1:p.Leu14=
NM_198407.2:c.42C>G MANE Select NP_940799.1:p.Leu14=
Search 100 bp 5'
Search 100 bp 3'